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	1.	Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: implication for molecular diagnosis. [electronic resource] by Ouragini, Houyem Haddad, Faten Darragi, Imen Abbes, Salem Producer: 20141231 In: Hematology (Amsterdam, Netherlands) vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level. [electronic resource] by Chaouch, Leila Sellami, Houssem Kalai, Miniar Darragi, Imen Boudrigua, Imen Chaouachi, Dorra Abbes, Salem Mnif, Samia Producer: 20200629 In: Journal of pediatric hematology/oncology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Hb Moscva [β24(B6)Gly→Asp (GGT>GAT), HBB: c.74G>A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient. [electronic resource] by Ghaber, Sidi M Trabelsi, Nawel Salem, Mohamed L Haddad, Faten Abba, Aminetou Darragi, Imen Abbes, Salem Producer: 20180921 In: Hemoglobin vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia. [electronic resource] by Chaouch, Leila Said, Yossra Moumni, Imen Mahjoubi, Imen Chaabene, Arij Ben Darragi, Imen Ghanem, Abderraouf Abbes, Salem Producer: 20130704 In: Annales de biologie clinique vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1. [electronic resource] by Chaouch, Leila Kalai1, Miniar Darragi, Imen Boudrigua, Imen Chaouachi, Dorra Ammar, Slim Ben Mellouli, F Bjaoui, M Abbes, Salem Producer: 20170302 In: Hematology (Amsterdam, Netherlands) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients. [electronic resource] by Chaouch, Leila Moumni, Imen Ouragini, Houyem Darragi, Imen Kalai, Miniar Chaouachi, Dorra Boudrigua, Imen Hafsia, Raouf Abbes, Salem Producer: 20170405 In: Hematology (Amsterdam, Netherlands) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients. [electronic resource] by Chaouch, Leila Moumni, Imen Ouragini, Houyem Darragi, Imen Kalai, Miniar Chaouachi, Dorra Boudrigua, Imen Hafsia, Raouf Abbes, Salem Publication details: Hematology (Amsterdam, Netherlands) Mar 2016 In: Hematology (Amsterdam, Netherlands) p. 1-5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients. [electronic resource] by Chaouch, Leila Kalai, Miniar Jbara, Manel Ben Chaabene, Arij Ben Darragi, Imen Chaouachi, Dorra Mallouli, Fethi Hafsia, Raouf Ghanem, Abderraouf Abbes, Salem Producer: 20161108 In: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients. [electronic resource] by Kalai, Miniar Dridi, Marwa Chaouch, Leila Moumni, Imen Ouragini, Houyem Darragi, Imen Boudrigua, Imen Chaouachi, Dorra Mellouli, Fethi Bejaoui, Mohamed Abbes, Salem Producer: 20170406 In: Hematology (Amsterdam, Netherlands) vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome. [electronic resource] by Haddad, Faten Trabelsi, Nawel Chaouch, Leila Darragi, Imen Oueslati, Meriem Boudriga, Imen Chaouachi, Dorra El-Borgi, Wijdene Hafsia, Raouf Abbes, Salem Ouragini, Houyem Producer: 20171219 In: Hemoglobin vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)